The proline 12 alanine substitution in the PPARgamma2 gene is associated with increased extent of coronary artery disease in men

Exp Clin Endocrinol Diabetes. 2009 Oct;117(9):519-21. doi: 10.1055/s-0029-1216351. Epub 2009 Jun 17.

Abstract

Objective: To determine whether there is an independent association between the Pro12Ala polymorphism in the peroxisome proliferator-activated-receptor gamma2 (PPARgamma2)-gene and the extent of coronary artery disease in men.

Research design and methods: We determined the Pro12Ala polymorphism in the PPARgamma2 gene in 240 male patients undergoing elective coronary angiograpy, and quantitated the degree of CAD by evaluating the extent-score which better correlates with known risk factors than other measures of CAD.

Results: The presence of the 12Ala allele was significantly associated with higher CAD extent (r=0.27, p<0.01). CAD extent was also correlated with the extent of insulin resistance (HOMA, r=0.22, p<0.01), and age (r=0.16, p<0.05). Multivariate analysis revealed an independent association between the 12Ala allele PPARgamma2 with extent-score (beta=0.32, p<0.01).

Conclusions: The 12Ala allele in PPARgamma2 correlates with a significantly increased CAD extent in men, which suggest that lower activity of the transcription factor PPARgamma2 is associated with more severe CAD.

MeSH terms

  • Age Factors
  • Aged
  • Alanine / genetics
  • Alleles
  • Angiography
  • Coronary Artery Disease / genetics*
  • Gene Frequency / genetics
  • Genetic Predisposition to Disease*
  • Genotype
  • Humans
  • Insulin Resistance / genetics
  • Male
  • Middle Aged
  • PPAR gamma / genetics*
  • Polymorphism, Genetic / genetics*
  • Proline / genetics
  • Protein Isoforms / genetics
  • Regression Analysis

Substances

  • PPAR gamma
  • Protein Isoforms
  • Proline
  • Alanine